Elsevier
Tetrahedron Letters
,  volume 45 ,  issue 46 ,  pages 8461-8463

An asymmetric dihydroxylation route to (2S,3S)-3-hydroxypipecolic acid

Publication type: Journal Article
Publication date: 2004-11-01
Elsevier
scimago Q3
wos Q3
SJR: 0.334
CiteScore: 3.2
Impact factor: 1.5
ISSN: 00404039, 18733581
Organic Chemistry
Drug Discovery
Biochemistry
Abstract
A concise enantioselective synthesis of (2S,3S)-3-hydroxypipecolic acid 1 starting from 1,4-butanediol using Sharpless asymmetric dihydroxylation and the regioselective nucleophilic opening of a cyclic sulfate as the key steps is described.
Found 
Found 

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GOST |
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GOST Copy
Bodas M. S., Kumar P. An asymmetric dihydroxylation route to (2S,3S)-3-hydroxypipecolic acid // Tetrahedron Letters. 2004. Vol. 45. No. 46. pp. 8461-8463.
GOST all authors (up to 50) Copy
Bodas M. S., Kumar P. An asymmetric dihydroxylation route to (2S,3S)-3-hydroxypipecolic acid // Tetrahedron Letters. 2004. Vol. 45. No. 46. pp. 8461-8463.
RIS |
Cite this
RIS Copy
TY - JOUR
DO - 10.1016/j.tetlet.2004.09.123
UR - https://doi.org/10.1016/j.tetlet.2004.09.123
TI - An asymmetric dihydroxylation route to (2S,3S)-3-hydroxypipecolic acid
T2 - Tetrahedron Letters
AU - Bodas, Mandar S.
AU - Kumar, Pradeep
PY - 2004
DA - 2004/11/01
PB - Elsevier
SP - 8461-8463
IS - 46
VL - 45
SN - 0040-4039
SN - 1873-3581
ER -
BibTex |
Cite this
BibTex (up to 50 authors) Copy
@article{2004_Bodas,
author = {Mandar S. Bodas and Pradeep Kumar},
title = {An asymmetric dihydroxylation route to (2S,3S)-3-hydroxypipecolic acid},
journal = {Tetrahedron Letters},
year = {2004},
volume = {45},
publisher = {Elsevier},
month = {nov},
url = {https://doi.org/10.1016/j.tetlet.2004.09.123},
number = {46},
pages = {8461--8463},
doi = {10.1016/j.tetlet.2004.09.123}
}
MLA
Cite this
MLA Copy
Bodas, Mandar S., and Pradeep Kumar. “An asymmetric dihydroxylation route to (2S,3S)-3-hydroxypipecolic acid.” Tetrahedron Letters, vol. 45, no. 46, Nov. 2004, pp. 8461-8463. https://doi.org/10.1016/j.tetlet.2004.09.123.